Labeling and dosing error recalls
Nothing is contaminated in these recalls — the package says the wrong thing. That can mean a bottle holding a different strength than the label states, two products packed in the wrong carton, or missing directions. For medication these can matter as much as contamination, because the dose taken is the wrong one.
972 stored notices, reported between Jun 20, 2012 and Sep 23, 2026. Newest first.
Reported Jan 25, 2017
HCG (Chorionic Gonadotropin Lyopholized) II, 1000 unit vial, Rx only, Prepared by Town & Country, Compounding &…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Town and Country Compounding and Consultation Services, LLC
FDA (openFDA drug enforcement)
Reported Jan 18, 2017
i.v. Station and i.v. Station ONCO Automated Drug Compounding System, Pharmacy Compounding System Device Listing Number…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Health Robotics S.r.l.
FDA (openFDA device enforcement)
Reported Jan 18, 2017
Oxford Fixed Lateral Bearing Size F Right, Part Number 154375 Lot 744260, Sterile, The product is placed into an…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer Biomet, Inc.
FDA (openFDA device enforcement)
Reported Jan 4, 2017
INOVA (benzoyl peroxide) 4%, Easy Pad (tocopherol) 5%, For topical use only, packaged in a box containing: 30 pads of…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Cipher Pharmaceuticals US LLC
FDA (openFDA drug enforcement)
Reported Dec 28, 2016
Zeus-P Lumbar Interbody Device
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Amendia, Inc.
6 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 28, 2016
Hyoscyamine Sulfate, Sublingual Tablets, 0.125 mg, 100-count bottle, Rx only, Manufactured for: Virtus Pharmaceuticals…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Virtus Pharmaceuticals Opco Ii L
2 more products in this recall
FDA (openFDA drug enforcement)
Reported Dec 21, 2016
ellman A CYNOSURE COMPANY Minor Surgery Bipolar Cable, Contents: Five (5) Disposable Bipolar Cables,STERILE The Minor…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ellman International, Inc.
FDA (openFDA device enforcement)
Reported Dec 21, 2016
Clear plastic cup labeled as: The Farmers Market Buffalo Hot Peanuts; Net Wt. 5 oz.; UPC 3003499846; Best By 10/25/2016
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Giant Eagle, Inc.
FDA (openFDA food enforcement)
Reported Dec 14, 2016
Empowr Knee System Product Usage: Non-porous proximal tibial baseplate implants, utilized in either posterior cruciate…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Encore Medical, LP
FDA (openFDA device enforcement)
Reported Dec 14, 2016
UltraSeal XT Plus Clear Refill. The package contains 4x 1.2 ml UltraSeal XT Plus. Product Usage: The UltraSeal XT Plus…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ultradent Products, Inc.
FDA (openFDA device enforcement)
Reported Dec 14, 2016
SODIUM FERRIC GLUCONATE COMPLEX IN SUCROSE INJECTION, 62.5mg elemental iron/5mL, 10 (5mL vials) per shelf pack, Rx…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.West-Ward Pharmaceuticals Corp.
FDA (openFDA drug enforcement)
Reported Dec 7, 2016
ConforMIS iTotal Cruciate Retaining (CR) Knee Replacement System, Sterile Catalog Number: TCR-111-1111. Intended for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ConforMIS, Inc.
FDA (openFDA device enforcement)
Reported Nov 30, 2016
LEVOXYL(R) (levothyroxine sodium tablets, USP), 200 mcg, 100 count bottles, Rx only, Manufactured and Distributed by:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Pfizer Inc.
FDA (openFDA drug enforcement)
Reported Nov 22, 2016
H.J. Heinz Co. Recalls Products Incorrectly Labeled As Pork Gravy Due To Misbranding and Undeclared Allergens
High riskUsing this product could cause serious injury, illness or death — stop using it now.H.J. Heinz Co.
USDA FSIS
Reported Nov 16, 2016
SB Knife -Electrosurgical Knife, Sterile Size: Working Length 2.3M Maximum OD 2.6mm. Product Usage: The SB Knife is a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Akita Sumitomo Bakelite Co., Ltd.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Nov 16, 2016
Reprocessed Daig Steerable and Daig Supreme Fixed Curve Diagnostic Electrophysiology Catheters Model Numbers: 401940,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Sustainability Solutions
FDA (openFDA device enforcement)
Reported Nov 16, 2016
Kamedis BIO-HERBAL DANDRUFF CARE THERAPEUTIC 2-STEP DANDRUFF CARE SYSTEM - Kamedis Bio-Herbal Dandruff Care 0.1%…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Taro Pharmaceuticals U.S.A., Inc.
FDA (openFDA drug enforcement)
Reported Nov 16, 2016
Testosterone 200 mg/Anastrozole 9 mg Pellet, Compounded by: Wells Pharmacy Network
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Wells Pharmacy Network, LLC
6 more products in this recall
FDA (openFDA drug enforcement)
Reported Nov 9, 2016
Sodium Chloride Ophthalmic Solution, USP, 5%, 15 mL (0.5 fL oz.) bottle, Akorn, Inc., Lake Forest, IL 60045, NDC…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Akorn Inc.
FDA (openFDA drug enforcement)
Reported Nov 9, 2016
Select Recipe Buttermilk Ranch Dressing, Net contents: 1 GAL (3.79 L), 4 X 1 GAL
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Oasis Foods Co.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Nov 9, 2016
Gildess 1.5/30 (norethindrone acetate, 1.5 mg and ethinyl estradiol tablets, 0.03 mg, USP), 21 count, (a) 3 blisters…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Par Pharmaceutical, Inc.
4 more products in this recall
FDA (openFDA drug enforcement)
Reported Nov 2, 2016
DM Light Slices Yellow Cling Peaches -15 oz (425g) 300 x 407
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Del Monte Research Center - Walnut Creek
FDA (openFDA food enforcement)
Reported Oct 26, 2016
New Seasons Market Creamy Almond Butter 16oz; Label reads in part "***NEW SEASONS WILD FRIENDS FOODS PORTLAND, OR ***…
High riskUsing this product could cause serious injury, illness or death — stop using it now.New Seasons Market
FDA (openFDA food enforcement)
Reported Oct 26, 2016
Trokendi XR (topiramate) extended-release capsule, 50mg, 30-count blister pack, Rx only, Manufactured by: Catalent…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Supernus Pharmaceuticals, Inc.
FDA (openFDA drug enforcement)
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RecallNow is not a government agency. Every notice above was published by the FDA, USDA FSIS or CPSC and links back to its source. Browse the whole archive.